Huang Wei, Zhou Quan, Yuan Xia, Ge Ze-Mei, Ran Fu-Xiang, Yang Hua-Yu, Qiang Guang-Liang, Li Run-Tao, Cui Jing-Rong
1. State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
2. Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
J Cancer. 2016 Jun 6;7(9):1133-41. doi: 10.7150/jca.14519. eCollection 2016.
Cisplatin is one of the most common drugs used for treatment of solid tumors such as ovarian cancer. Unfortunately, the development of resistance against this cytotoxic agent limits its clinical use. Here we report that YSY01A, a novel proteasome inhibitor, is capable of suppressing survival of cisplatin-resistant ovarian cancer cells by inducing apoptosis. And YSY01A treatment enhances the cytotoxicity of cisplatin in drug-resistant ovarian cancer cells. Specifically, YSY01A abrogates regulatory proteins important for cell proliferation and anti-apoptosis including NF-κB p65 and STAT3, resulting in down-regulation of Bcl-2. A dramatic increase in cisplatin uptake was also observed by inductively coupled plasma-mass spectrometry following exposure to YSY01A. Taken together, YSY01A serves as a potential candidate for further development as anticancer therapeutics targeting the proteasome.
顺铂是用于治疗实体瘤(如卵巢癌)的最常用药物之一。不幸的是,对这种细胞毒性药物产生耐药性限制了其临床应用。在此我们报告,新型蛋白酶体抑制剂YSY01A能够通过诱导凋亡来抑制顺铂耐药卵巢癌细胞的存活。并且YSY01A处理增强了顺铂对耐药卵巢癌细胞的细胞毒性。具体而言,YSY01A消除了对细胞增殖和抗凋亡重要的调节蛋白,包括NF-κB p65和STAT3,导致Bcl-2下调。在暴露于YSY01A后,通过电感耦合等离子体质谱法还观察到顺铂摄取显著增加。综上所述,YSY01A作为靶向蛋白酶体的抗癌治疗药物有进一步开发的潜力。